Canonical Allele Identifier: PA2827957097
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 161206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met959Ile
CA007863
NM_001354897.2:c.2877G>T
CA16027540
NM_001354897.2:c.2877G>A
CA16027541
NM_001354897.2:c.2877G>C